Browse skills

Access and query a vast, specialized database of medical knowledge, research, and clinical data for insights.

Quickly retrieve relevant clinical trial details from databases based on patient criteria and research interests.

Retrieve clinically relevant genetic variant information, pathogenicity classifications, and supporting evidence from ClinVar.

Access and query Davila7's curated clinical pharmacogenomics (clincPGX) database for personalized medication guidance.

Provides database guidance and assistance for software development workflows.

Provides database guidance and assistance for software development workflows.

Queries ClinVar data via API to identify genetic variants, their classifications, and associated clinical significance.

Quickly searches and filters clinical trial databases for ovarian cancer patients based on specified criteria.

Quickly retrieve FDA approval status, clinical trial data, and regulatory information from the official FDA databases.

Accesses and analyzes clinical data from the PGX database to optimize patient treatment plans based on genetic insights.

Access and query clinical data from PGx databases via a structured interface powered by Jackspace's AI.

Automate Supabase project creation, deployment, and management tasks directly from your AI workflows with adaptationio's supabase-cli skill.

Access ClinVar variant information, including classifications and evidence, directly within Jackspace for streamlined genomic analysis.

Quickly find relevant clinical trials matching patient criteria using Jackspace's curated database of trial information.

Provides Supabase guidance and assistance for software development workflows.

Neo4J Cli Tools Skill — provides AI agent assistance for software development workflows.

Access and query Dr. Shailesh's curated clinical trial database for relevant studies based on patient criteria.

Access and query ClinVar data via drshailesh88's agent to retrieve variant information and clinical significance assessments.

Accesses and analyzes clinical pharmacogenomics data from drshailesh88's curated database for personalized medication insights.

Queries ClinVar to retrieve genetic variant information, including classifications, interpretations, and associated publications.

Accesses and retrieves clinical pharmacogenomics (PGx) data from a specialized database for personalized medication guidance.

Access and query a comprehensive clinical trials database to identify relevant studies based on patient criteria.

Connects, queries, and manipulates PostgreSQL databases using advanced AI techniques for efficient data management.

Access and query ClinVar variant data via a streamlined interface powered by microck's specialized AI.